A missense mutation in TUBD1 is associated with high juvenile mortality in Braunvieh and Fleckvieh cattle

BACKGROUND: Haplotypes with reduced or missing homozygosity may harbor deleterious alleles that compromise juvenile survival. A scan for homozygous haplotype deficiency revealed a short segment on bovine chromosome 19 (Braunvieh haplotype 2, BH2) that was associated with high juvenile mortality in B...

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Vydáno v:BMC Genomics
Hlavní autoři: Schwarzenbacher, Hermann, Burgstaller, Johann, Seefried, Franz R., Wurmser, Christine, Hilbe, Monika, Jung, Simone, Fuerst, Christian, Dinhopl, Nora, Weissenböck, Herbert, Fuerst-Waltl, Birgit, Dolezal, Marlies, Winkler, Reinhard, Grueter, Oskar, Bleul, Ulrich, Wittek, Thomas, Fries, Ruedi, Pausch, Hubert
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2016
Témata:
Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4880872/
https://ncbi.nlm.nih.gov/pubmed/27225349
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-016-2742-y
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